Deviation Supervisor - Onsite Greenville, Nc

PPD (Thermo Fisher) UK

Greenville, NC, US
Onsite
Cgmp compliance adherence
Root cause analysis tools
Capa initiation and oversight
This role involves leading a team to conduct thorough investigations and ensure timely completion of corrective actions in a high-volume sterile manufacturing facility

Job Summary

  • This role involves leading a team to conduct thorough investigations and ensure timely completion of corrective actions in a high-volume sterile manufacturing facility.
  • The position requires expertise in using root cause analysis tools like TapRooT and Fishbone diagrams to identify assignable causes for deviations.
  • Candidates must possess strong critical thinking skills to assess quality impacts on patients and products while adhering to regulatory guidelines.

Matching Summary

This role involves leading a team to conduct thorough investigations and ensure timely completion of corrective actions in a high-volume sterile manufacturing facility.

Skills & Requirements

Must-have

  • cGMP compliance adherence
  • Root Cause Analysis tools
  • CAPA initiation and oversight
  • Deviation investigation leadership
  • Technical writing for reports

Nice-to-have

  • Cross-functional collaboration skills
  • Statistical data analysis ability
  • Conflict resolution in teams
  • Mentoring and training staff
  • Project management prioritization

Key Requirements

  • Bachelor's Degree in Science or Engineering
  • Minimum 5 years cGMP experience
  • Minimum 3 years technical writing experience
  • Proficiency with Track Wise software
  • Experience with TapRooT or similar tools

Work Rights

Not specified

Tailored Resume

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